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Ophthalmic Genetics|August 2, 2023
The genetic counselor workforce in inherited retinal disease clinics: a descriptive assessmentMichelle Alabek, Katherine Andersen, Lesley Everett, et al.Journal of Genetic Counseling|July 23, 2024
Genetic counselors' awareness and attitudes regarding gene therapiesChelsey Walsh, Andrea L Durst, Damara Ortiz, et al.Research Square|April 22, 2024
Recurrent Retinal Detachment in Stickler SyndromeTimothy Chen, Marjan Fooladi, Michelle Alabek, et al.Case Reports in Ophthalmology|June 19, 2025
Exclusively Macular Phenotype of Non-Syndromic <i>MFSD8</i>-Related Disease: A Case ReportSean Ghiam, Ryan Zukerman, Morgan Brzozowski, et al.Eye (London, England)|October 18, 2024
Recurrent retinal detachment in Stickler SyndromeTimothy H Chen, Marjan Imani Fooladi, Michelle Alabek, et al.Cornea|December 1, 2022
Congenital Corneal Opacity in 22q11.2 Deletion Syndrome: A Case SeriesElena Franco, Naeem Iqbal, Parth R Shah, et al.Retina (Philadelphia, Pa.)|May 13, 2025
Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of LiteratureSamer Khateb, Sean Ghiam, Jordan Safran, et al.Ophthalmology Science|May 27, 2026
Association of Autosomal Dominant Snowflake Vitreoretinal Degeneration with RetinoschisisBikash R Pattnaik, Ken K Nischal, Oleg Alekseev, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 5, 2020
Developing a pediatric ophthalmology telemedicine program in the COVID-19 crisisSaloni Kapoor, Amgad Eldib, Jamila Hiasat, et al.NPJ Genomic Medicine|April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypesRyan E Schmidt, Amy E Pohodich, David Birch, et al.Pageof 1